Beker Merve, Bolat Busenur, Johnson Bahar Sarikamis, Ercin Nilufer, Cakmak Rabia Kalkan, Kaya Sare B, Besli Nail, Celik Ulkan, Beker Mustafa C
Department of Medical Biology, International School of Medicine, University of Health Sciences Turkiye, Istanbul, Turkiye;
Department of Physiology, Institute of Health Sciences, Yeditepe University, Istanbul, Turkiye.
In Vivo. 2025 Jul-Aug;39(4):2050-2065. doi: 10.21873/invivo.14000.
BACKGROUND/AIM: Biological aging refers to the progressive deterioration of an organism's functions due to accumulated cellular and molecular damage. NeuroD2, a critical transcription factor, plays a crucial role in neuronal development and synaptic maturation. This study investigates the role of NeuroD2 in hippocampal neuron organization, focusing on hilar mossy cells during aging, and employs bioinformatics to identify NeuroD2 targets linked to cellular aging.
We used 21 adult C57Bl/6 mice, categorized into three age groups: young (2 months), old (12 months), and very old (24 months). Mice were administered BrdU intraperitoneally for three consecutive days, 10 days before euthanasia. The brains were harvested and analyzed using immunofluorescence, Western blotting, and quantitative real-time PCR to evaluate NeuroD2 expression and associated signaling pathways in hippocampal tissue. Additionally, bioinformatics analysis was performed using two open-access datasets (ProteomeXchange Consortium, Dataset identifier: PXD043352; Gene Expression Omnibus, GEO: GSE67539) and to explore potential interactions between NeuroD2 targets and biological aging components.
Our results revealed that NeuroD2 expression changed significantly with age and correlated with AKT signaling. Moreover, we identified a potential link between NeuroD2 activity and the AKT pathway, indicating NeuroD2's role in mitigating aging-related stress. Bioinformatics analysis identified 513 down-regulated and 638 up-regulated proteins, with NeuroD2 targets involved in axonal projection showing increased expression in older mice. Contrary to expectations, pathway enrichment analysis highlighted axon guidance molecules rather than oxidative stress markers.
This study underscores NeuroD2's critical role in preserving hippocampal integrity and reveals molecular mechanisms underlying age-related neuronal changes. Our findings provide insights into the role of NeuroD2 in regulating key pathways during healthy aging, potentially mitigating the impacts of aging.
背景/目的:生物衰老指的是由于细胞和分子损伤的积累导致生物体功能的逐渐衰退。NeuroD2作为一种关键的转录因子,在神经元发育和突触成熟过程中发挥着至关重要的作用。本研究调查了NeuroD2在衰老过程中对海马神经元组织的作用,重点关注门区苔藓细胞,并运用生物信息学方法来识别与细胞衰老相关的NeuroD2靶点。
我们使用了21只成年C57Bl/6小鼠,分为三个年龄组:年轻组(2个月)、老年组(12个月)和高龄组(24个月)。在安乐死10天前,连续三天给小鼠腹腔注射BrdU。采集小鼠大脑,采用免疫荧光、蛋白质免疫印迹法和定量实时聚合酶链反应来评估海马组织中NeuroD2的表达及相关信号通路。此外,利用两个开放获取数据集(蛋白质组交换联盟,数据集标识符:PXD043352;基因表达综合数据库,GEO:GSE67539)进行生物信息学分析,以探索NeuroD2靶点与生物衰老成分之间的潜在相互作用。
我们的结果显示,NeuroD2的表达随年龄显著变化,且与AKT信号传导相关。此外,我们确定了NeuroD2活性与AKT通路之间的潜在联系,表明NeuroD2在减轻衰老相关应激方面的作用。生物信息学分析确定了513种下调蛋白和638种上调蛋白,参与轴突投射的NeuroD2靶点在老年小鼠中表达增加。与预期相反,通路富集分析突出了轴突导向分子而非氧化应激标志物。
本研究强调了NeuroD2在维持海马完整性方面的关键作用,并揭示了与年龄相关的神经元变化的分子机制。我们的发现为NeuroD2在健康衰老过程中调节关键通路的作用提供了见解,可能减轻衰老的影响。